Ligustrone B

Details

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Internal ID 11fba738-9d6a-420b-835f-9889ab5b74b6
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name 5-hydroxy-11-methoxy-2-methyl-8,9-dihydroindeno[5,6-h]chromene-4,10-dione
SMILES (Canonical) CC1=CC(=O)C2=C(O1)C3=C(C4=C(CCC4=O)C=C3C=C2O)OC
SMILES (Isomeric) CC1=CC(=O)C2=C(O1)C3=C(C4=C(CCC4=O)C=C3C=C2O)OC
InChI InChI=1S/C18H14O5/c1-8-5-12(20)16-13(21)7-10-6-9-3-4-11(19)14(9)17(22-2)15(10)18(16)23-8/h5-7,21H,3-4H2,1-2H3
InChI Key PAPDLIMQTJVGKM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H14O5
Molecular Weight 310.30 g/mol
Exact Mass 310.08412354 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.10
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ligustrone B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9811 98.11%
Caco-2 + 0.6809 68.09%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8175 81.75%
OATP2B1 inhibitior - 0.5764 57.64%
OATP1B1 inhibitior + 0.9186 91.86%
OATP1B3 inhibitior + 0.9852 98.52%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8218 82.18%
P-glycoprotein inhibitior - 0.6883 68.83%
P-glycoprotein substrate - 0.8549 85.49%
CYP3A4 substrate + 0.5528 55.28%
CYP2C9 substrate - 0.5701 57.01%
CYP2D6 substrate - 0.8122 81.22%
CYP3A4 inhibition - 0.7197 71.97%
CYP2C9 inhibition - 0.5615 56.15%
CYP2C19 inhibition + 0.5072 50.72%
CYP2D6 inhibition - 0.7524 75.24%
CYP1A2 inhibition + 0.9385 93.85%
CYP2C8 inhibition - 0.6397 63.97%
CYP inhibitory promiscuity - 0.7284 72.84%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6933 69.33%
Eye corrosion - 0.9774 97.74%
Eye irritation - 0.6386 63.86%
Skin irritation - 0.7869 78.69%
Skin corrosion - 0.9622 96.22%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5937 59.37%
Micronuclear + 0.5159 51.59%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.9153 91.53%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.4891 48.91%
Acute Oral Toxicity (c) III 0.5161 51.61%
Estrogen receptor binding + 0.6938 69.38%
Androgen receptor binding + 0.6628 66.28%
Thyroid receptor binding - 0.7087 70.87%
Glucocorticoid receptor binding + 0.7410 74.10%
Aromatase binding + 0.5812 58.12%
PPAR gamma + 0.8874 88.74%
Honey bee toxicity - 0.8847 88.47%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.6635 66.35%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.68% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.51% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.24% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 93.27% 91.49%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.24% 93.99%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.77% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.81% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.03% 86.33%
CHEMBL2581 P07339 Cathepsin D 88.46% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 87.74% 94.73%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 83.30% 96.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.26% 96.21%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.03% 93.65%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.01% 85.14%
CHEMBL2535 P11166 Glucose transporter 82.90% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.08% 99.17%
CHEMBL4581 P52732 Kinesin-like protein 1 81.68% 93.18%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.49% 99.15%
CHEMBL4208 P20618 Proteasome component C5 80.36% 90.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 71438742
LOTUS LTS0015069
wikiData Q75062633